EP0540324A2 - Von Luft gestützte alkalische Zellen und dazugehörige Dichtungsanordnung - Google Patents

Von Luft gestützte alkalische Zellen und dazugehörige Dichtungsanordnung Download PDF

Info

Publication number
EP0540324A2
EP0540324A2 EP92309902A EP92309902A EP0540324A2 EP 0540324 A2 EP0540324 A2 EP 0540324A2 EP 92309902 A EP92309902 A EP 92309902A EP 92309902 A EP92309902 A EP 92309902A EP 0540324 A2 EP0540324 A2 EP 0540324A2
Authority
EP
European Patent Office
Prior art keywords
cell
layer
air
cell according
layers
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP92309902A
Other languages
English (en)
French (fr)
Other versions
EP0540324A3 (en
EP0540324B1 (de
Inventor
Robert James Hyland
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Edgewell Personal Care Brands LLC
Original Assignee
Eveready Battery Co Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Eveready Battery Co Inc filed Critical Eveready Battery Co Inc
Publication of EP0540324A2 publication Critical patent/EP0540324A2/de
Publication of EP0540324A3 publication Critical patent/EP0540324A3/en
Application granted granted Critical
Publication of EP0540324B1 publication Critical patent/EP0540324B1/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M12/00Hybrid cells; Manufacture thereof
    • H01M12/02Details
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/30Arrangements for facilitating escape of gases
    • H01M50/342Non-re-sealable arrangements
    • H01M50/3425Non-re-sealable arrangements in the form of rupturable membranes or weakened parts, e.g. pierced with the aid of a sharp member
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/30Arrangements for facilitating escape of gases
    • H01M50/394Gas-pervious parts or elements
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Definitions

  • the present invention relates to air-assisted alkaline cells having an improved seal assembly.
  • Alkaline cells are well known in the art, and they typically include a zinc anode, manganese dioxide as the cathode and an aqueous solution of potassium hydroxide forthe electrolyte. These cells are commercially available for use both in industry and in the home.
  • a new type of alkaline cell has, however, recently been disclosed by the Spanish Company, Ce- gasa International.
  • the new cell which is referred to as an air-assisted cell, is designed to use oxygen in the air to "re-charge" the cathode.
  • the cell employs the same basic components as the conventional alkaline cell, but it is designed so that the positive electrode containing the manganese dioxide (Mn0 2 ) is supported about its periphery and along its full length in the cell by a perforated ribbed air distribution grid.
  • the bottom or negative end of the cell then has an insulating support which allows air to enter the cell and pass up along the outside of the supported positive electrode.
  • the electrochemical reaction depends primarily upon the presence of the manganese dioxide cathode. As the reaction progresses, and the manganese dioxide cathode is electrochemically reduced, air within the cell re-oxidizes and re-charges the manganese dioxide. This re-charging of the manganese dioxide means that the fixed quantity of manganese dioxide in the cathode may be discharged and then re-charged numerous times, and thus that the quantity of manganese dioxide in the cathode is not limiting upon the lifetime of the cell.
  • the manganese dioxide in the cathode is reduced to a lower oxidation state.
  • the discharged active manganese dioxide cathode then undergoes a reaction with the air which is already in, or which enters, the cell to re-oxidize the reduced cathode such that the cathode becomes re-charged.
  • the oxygen in the air will spontaneously restore or regenerate the higher oxidation state over a period of time. If the cell is subjected to brief periods of high rate discharge, it must then be rested for substantial periods of time between each discharge to enable the Mn0 2 to be completely re-charged.
  • the air re-charges the Mn0 2 as quickly as it is discharged.
  • the ability of the cathode to be re-charged is limited only by its access to air.
  • the cathode material is regenerated without involving the zinc anode material which is oxidized during the discharge but cannot be regenerated during a rest period. In view of this, less cathode material needs to be added to an air-assisted alkaline cell and, in turn, the volume of zinc may be increased in the cell to increase the overall capacity of the cell, without increasing the overall volume of the cell.
  • the ampere hour output of a cathode in a standard alkaline battery is limited by the quantity of manganese dioxide incorporated in the cell when the cell is manufactured.
  • the maximum service which is obtainable is greater for the air-assisted cell than for the standard alkaline cell.
  • a further desirable feature for incorporation into a seal for any cell is a safety vent which will rupture and release the pressure inside the cell when this pressure exceeds a predetermined value.
  • US-A-5,051,323 describes a polymeric seal for an air-asisted alkaline cell, which seal has holes in it to allow for entry of air.
  • the seal member consists of a gasket formed from a plastics material, a metal washer and a metal cap in which the holes are present.
  • an object of the present invention to provide a seal for an air-assisted cell, which seal may effectively permit air to enter the cell whilst preventing electrolyte from leaving the cell, which seal also functions as a safety vent.
  • the present invention provides an air-assisted alkaline cell having a seal assembly including a seal member so configured as to retain an air-permeable multi-layer plastics film, characterised in that the multi-layer plastics film comprises at least three layers of a plastics material, an inner layer being of a plastics material different from and having a higher melting point than the outer layers, said at least three layers being heat sealed at the peripheries thereof.
  • the seal assembly itself provides a safety vent for the cell.
  • the multi-layer plastics film comprises at least three layers of plastics material.
  • the exact number of layers in the film is not essential to the present invention, although the choice of the number of layers may be influenced by the characteristics of the plastics material chosen, for example the thickness of the material and its permeability properties. Generally, we find that a total of three layers is satisfactory, although a multi-layer film comprising two or more inner layers, i.e. a total of four or more layers, is preferred.
  • the overall thickness of the multi-layer film, and the thicknesses of the individual component layers, depends on various factors, such as the number of layers from which the multi-layer film is formed, the choice of material for the layers and the particular size and cell system employed.
  • the multi-layer film must be sufficiently thick to prevent undesirable materials, such as the electrolyte, from leaving the cell, but its thickness must not be so great that it is unable to rupture when the internal pressure of the cell exceeds a predetermined value.
  • the thicknesses of the individual component layers may also vary, and it is not essential that these layers are all of the same thickness. It is preferred that the thickness of each of the outer layers of the film varies between 0.5 mil [0.0127 mm] and 6 mils [0.1524 mm], preferably 1 mil [0.0254 mm] to 4 mils [0.1016 mm].
  • Afeature which may influence the thickness of an inner layer may be the ability of such a layer to rupture when the pressure inside the cell exceeds a predetermined value, as a single layer of a certain thickness may be too strong to rupture when the pressure exceeds that value. In such cases, it is generally recommended to use two or more inner layers, each layer being of a lesser thickness than that of a single thick layer, and adding up to the desired thickness.
  • each inner layer is of from 1 mil [0.0254 mm] to 10 mils [0.254 mm] thick, although more preferably, each inner layer is from 3 mils [0.076 mm] to 5 mils [0.127 mm] thick.
  • the material from which the outer layers and an inner layer are made are different from each other, and have different melting points.
  • the outer layers both have a higher melting point than an inner layer.
  • the two outer layers may be made from different plastics materials, it is preferred that these two layers are made from the same material so that successful welding of these films at specific areas will ensure an assembled multi-layer film which is particularly suitable for use as an air-permeable seal in an air-assisted cell.
  • the two outer layers are made from a different material, it is not essential for these materials to have the same melting point, so long as the melting point of each layer is lower than that of the inner layer(s). It is, however, preferred that these two layers are formed from materials which do have the same melting point.
  • Each outer layer may, if desired, consist of two or more sub-layers, although it is preferred that each outer layer is formed from a single layer.
  • the inner layer or, when there is more than one inner layer, each inner layer, is made from a different material from the outer layers.
  • these inner layers may themselves be made from different materials and these materials may have different melting points. It is preferred, however, that when there is more than one inner layer, the inner layers are made from the same plastics material having the same melting point.
  • the multi-layer plastics film is formed by heat sealing the layers at the peripheries thereof. Any suitable technique for heat sealing may be used, so long as this only results in sealing at the peripheries of the layers. In general, we find that ultrasonic welding is the most preferred technique.
  • the two outer layers are of a material having the same melting point, which melting point is lower than that of an inner layer.
  • heat sealing e.g. welding
  • the two outer layers at the peripheries thereof will cause those layers to melt and to permeate the inner layer(s) of film at the heated areas.
  • the inner layer(s) will not melt because it will have a higher melting point.
  • an integral bond is one which is obtained from the flow of the melted outer layers towards each other, followed by solidification of the melted areas to form a solid unit.
  • the material from which the layers are made must be air-permeable and, in particular, the inner film must retard penetration of electrolyte, whilst simultaneously permitting air to pass through.
  • the material must also be impermeable to liquids such as the electrolyte used in the cell, for example potassium hydroxide.
  • a plastics film having only one component layer which is impermeable to electrolyte would fulfil the requirements of the present invention, forex- ample a film in which the inner layer(s) only is so impermeable, it is preferred that each of the layers possesses this characteristic.
  • the inner layer(s) is preferably constructed from a material having a series of interconnected crevices and/or small pores.
  • This construction allows the flow of selected gases and liquids to be controlled, and is also advantageous for the formation of the multi-layer plastics film in that the construction will allow a flowable material, such as the melted material of the two outer layers, to traverse from one side of the inner layer(s) to the other. Because the inner layer(s) has a higher melting point than the outer layers, the pores existing in the structure will not collapse when the multi-layer film is subjected to temperatures which will melt the outer layers.
  • Plastics materials which are suitable for formation of the outer layers include air-permeable polyalkylenes, particularly polypropylene, and those which are suitable for formation of the inner layer(s) include air-permeable polytetrahaloalkylenes, such as polytetrafluoroethylene.
  • Particularly suitable for the outer layers is the polypropylene film Celgard 4400 TM , which is a trademark for a product commercially available from Hoechst Celanese Corp., of Somerville, New Jersey, USA. This product is particularly suitable because it is a polypropylene film made by heat bonding an open mesh of polypropylene, of 3 mils [0.076 mm] thickness, to a solid layer of polypropylene of 1 mil [0.0254 mm] thickness. The open mesh provides structural strength to the film whilst the solid layer is available for bonding to another polypropylene surface.
  • the seal assembly itself provides a safety venting function. It is preferred in this embodiment that the plastics materials from which the multi-Iayerfilm is made are so chosen as to allow for rupture if the internal pressure of the cell exceeds a predetermined value. Features which affect this rupture may be, as discussed above, the number and thickness of the individual layers, and the choice of materials. In particular, the selection of the number of inner layers may affect the ability of the film to rupture. When in use, it is generally preferred that the multi-layer film will expand upwards and outwards when the pressure within the cell exceeds a predetermined value, finally rupturing to release that pressure. In an alternative embodiment, the individual layers of the multi-layer film may be so designed as to promote easy rupture under internally abusive conditions.
  • the top film may include a spoked wheel configuration, a mesh configuration or may be designed to have openings at certain intervals.
  • the inner film will be able to balloon upwards through the openings in the top film without undue restriction, thereby aiding venting.
  • the seal assembly includes a seal member which is so configured as to retain an air-permeable multi-layer plastics film. It is preferred that this seal member is constructed from an organic polymeric material, such as polypropylene.
  • the seal member should also be so configured as to allow the passage of airtherethough and this may be achieved, for example, by provision of at least one hole in the seal member.
  • the present invention provides an air-assisted cell comprising the active components of the cell including an electrolyte, all housed within a container closed by a cover having at least one opening, and said cover associated with a seal assembly comprising an organic polymeric seal member having a base with at least one opening and a multi-layer plastic film disposed onto the base, said multi-layer plastic film comprising at least one inner layer of a first plastic film sandwiched between two outer layers of a different type of plastic film with said two outer layers having substantially the same melting temperature and said melting temperature being lower than the melting temperature of the at least one inner layer of the first plastic film; said two outer layers and said at least one inner layer being porous to permit air to pass through with said inner layer preventing the passage of the cell's electrolyte; said multi-layer film heat sealed at least at its peripheral area so that said two outer layers form an integral bond through said inner layer at the peripheral area thereby permitting air to enter through the opening in the cover and through the multi-layer film into the cell and said multi-layerfilm
  • the seal member is so configured as to retain the multi-layer plastics film.
  • the multi-layer plastics film may fit inside, or be disposed onto, the seal member.
  • the seal member may consist of a substantially flat base surrounding an inner upstanding wall, which wall defines an opening, and a peripheral upstanding skirt. At least one opening in the base should then be present to permit air to flow into the cell.
  • the multi-layer plastics film in this arrangement may have an opening at its centre to accommodate the inner upstanding wall, i.e. so that it could be disposed onto the base member between the inner upstanding wall and the peripheral skirt. The multi-layer film may then, if desired, be physically retained within the seal member, e.g.
  • a fatty acid polyamide adhesive such as the type disclosed in U.S.
  • Patent 3,922,178 may if desired be used to reinforce the weld and to prevent creepage of electrolyte between the seal member and the air-permeable multi-layer film. Yet a further method for this retention is to provide concentric raised inner and outer ridges on the outer wall and/or the base of the seal member, such that the multi-layer plastics film is secured between the ridges.
  • a neutral cover having at least one opening may be placed over the multi-layerfilm.
  • An external cover with at least one opening may then be placed over the neutral cover and secured to the container of the cell through the use of the peripheral skirt of the seal memeber.
  • the cathode in the air-assisted cell of the present invention is suitably made from manganese dioxide, although any other cathode material which is rechargeable by air during operation of the cell would be appropriate.
  • a good source of highly porous manganese dioxide is the so-called chemically synthesized manganese dioxide or CMD.
  • CMD is usually marketed with a porosity of 25% to 35%.
  • CMD may be prepared in the form of spheres with high porosity, for example of approximately 60%. These porous spheres are advantageous in that they have a large surface area which is available for reaction with oxygen in an air-assisted cell.
  • substantially solid Mn0 2 In order to increase the total energy capacity of an air-assisted cell in an air-free environment, substantially solid Mn0 2 must be available for the cell reaction.
  • Agood source of substantially solid Mn0 2 is electrolytically deposited Mn0 2 , or EMD.
  • EMD may be obtained in the form of dense particles after the electrolytically deposited material is stripped from the electrodes, crushed and screened.
  • EMD has a porosity of approximately 10% - 16% and is, therefore, a substantially solid material. As the ratio of EMD to CMD increases, the air-free capacity of the cell also increases.
  • the amount of CMD and EMD used in the cathode of the cell depends on the desired parameters of the cell with, for example, more or less CMD being used per cathode depending on the energy capacity desired in the presence of air.
  • the air-assisted alkaline cell 2 is assembled in a conventional conductive steel container 4 which also forms an external terminal for the cell.
  • the cathode 6 for the cell 2 is preferably porous manganese dioxide for example CMD and/or EMD as described above..
  • the cathode 6 is formed in the container 4 a separator 8 is added to isolate the anode material 10 physically from the cathode 6 and the container 4, while still permitting ion transport between the electrodes.
  • the anode mix 10 is then added to the separator lined cavity of the cell.
  • the anode mix 10 comprises a mixture of zinc powder, a gel forming binder and a liquid electrolyte used in the cell.
  • the preferred binder is Carbopol 940 which is a carboxy polymethylene polymer available from the B. F. Goodrich Company, of Cleveland, Ohio, USA.
  • the preferred electrolyte is an aqueous solution of potassium hydroxide and is suitably an approximately 34% to 37% by weight solution of potassium hydroxide in water.
  • the electrolyte from the anode mix 10 permeates the separator 8, and the cathode 6.
  • An open area 12 is left in the cell to provide room for expansion of the anode mix 10.
  • a sub-assembly is used to close the cell.
  • the sub-assembly 20 consists of an anode current collector 22, a seal member 24, a multi-layer film 26, a neutral cover 28 and a rivet 30 which is used to join the several pieces together.
  • the anode current collector 22 is made from an electrically conducting metal that is inert to the caustic environment within the cell.
  • the metal from which the collector is made is preferably sheet brass.
  • the anode current collector 22 is rolled to have an arcuate shape with a top flat surface 32 which fits tightly against the bottom of the seal member 24. A nail or pin shaped collector would also be suitable.
  • the seal member 24 is made of an organic polymeric material which is compatible with the components of the cell.
  • the preferred material is polypropylene.
  • the seal member24 has a substantially flat bottom portion 33 surrounding an inner upstanding wall 34. Below and in line with the periphery of the bottom portion 33 is a substantially circular projecting first wall portion 36.
  • a plurality of circumferentially spaced spokes 38 extend from the periphery of the bottom portion 33 out to and below a peripheral upstanding wall 40 extending upwardly away from bottom portion 33.
  • the open spaces 42 between the spokes 38 provide a passage for air to pass through the seal member 24.
  • a multi-layer film 26 fits within the area of the seal member 24 bounded by the wall 34 and wall 40.
  • the multi-layer film 26 is made of two layers of polytetrafluoroethylene 44 sandwiched between two layers of an organic polymeric material, such as polypropylene, 46.
  • the multi-layer film 26 is ultrasonically welded at peripheral area 48 and inner area 50 to produce a sealed multi-layer assembly.
  • the top layer 46 could have spaced apart openings to permit the inner film 44 to expand with minimum resistance or restriction.
  • the multi-layer film 26 may be fastened to the bottom 33 and the spokes 38 by welding, if desired.
  • the multi-layer film 26 may be disposed onto the bottom 33 and then the layers of the multi-layer film 26 may be secured together and to the bottom 33 and spokes 38 by welding, preferably, ultrasonic welding.
  • a fatty polyamide adhesive may then be used to reinforce the weld and to prevent creepage of electrolyte between the seal member 24 and the air-permeable multi-layer film 26.
  • Two beads of the adhesive may be used such that one bead is placed around the periphery of the bottom 33 where it joins the inside of peripheral wall 40 and the second bead is placed on the bottom 33 where it joins the inner upstanding wall 34.
  • concentric raised inner and outer ridges 52 may be formed on the bottom 33 of the seal member 24. If desired and although not shown two inner ridges and two outer ridges may be formed on the bottom 33 of seal member 24.
  • the multi-layer film 26 will then be secured between the ridges 52 on the bottom 33 and the neutral cover 28.
  • the vented neutral cover 28 is preferably made of stainless steel and has at least one pair of spaced apertures 54 therein to allow the passage of air into the cell. The vented neutral cover 28 will fit within the area of the seal member 24 bounded by the peripheral wall 40.
  • the rivet 30 is preferably made of brass and has a thinned portion 56 which may be easily spread to bind all of the parts of the sub-assembly 20 together as shown in Figure 1.
  • the dimensions of the several components of the sub-assembly 20 and of the overall cell may be varied to meet the particular size requirements for the type of cell being assembled.
  • the sub-assembly 20 is inserted into the bottom of the inverted cell as shown in Fig. 1.
  • the wall 36 moves the top edge of the separator 8 toward the cathode material 6.
  • the wall 36 and separator 8 protect the anode mix 10 from contact with the air entering the cell. This avoids the loss of zinc due to direct reaction with oxygen.
  • the peripheral wall 40 of the seal member 24 insulates the neutral cover 28 from electrical contact with the container 4.
  • a bottom cover 58 is placed into the steel container4 and is then electrically insulated from contact with the container 4 by the peripheral wall 40 of seal member 24.
  • the bottom cover 58 makes electrical contact with the rivet 30, or other suitable electrically conductive means, enabling the bottom cover 58 to become the second external terminal for cell 2.
  • the edge of the steel container4, and of the wall 40 of sub-assembly 20 are then rolled to hold the upturned portion 60 of the bottom cover 58 locked in position on the bottom of the cell 4.
  • a gap 62 surrounds the bottom cover 58, separating it from contact with the container 4.
  • the bottom cover 58 contains three small apertures 64, one of which is shown in Fig. 1, spaced approximately 120° apart, which provide a passage for air to enter into the bottom of the cell 2.
  • the air may pass through the sub-assembly 20 and contact the top portion of the cathode 6 through the air passage 42.
  • the top cover 66 may be fastened to the container by welds 68 after the cathode is rammed into place. It may be added before or after this step as it is merely attached to the container 4.
  • Figs. 3 and 4 show another embodiment of the present invention utilising a seal assembly of a different design.
  • Figs. 3 and 4 show an air-assisted alkaline cell 3 that employs several of the same components shown in cell 2 of Fig. 1 and these components are identified with the same reference numbers.
  • a sub-assembly 5 as shown in Fig. 4 is used to close cell 3 as shown in Fig. 3.
  • the sub-assembly 5 consists of an anode current collector nail 7 made from an electronically conducting metal.
  • a seal member 9 is made of an organic polymeric material which is compatible with the components of cell 3, with the preferred material being polypropylene.
  • the seal member 9 has a substantially flat bottom portion 11 surrounding an upstanding inner wall 13.
  • a plurality of circumferentially spaced spokes 17 extend from the periphery of the bottom portion 11 out to and below a peripheral upstanding wall 19 extending upwardly away from bottom portion 11.
  • the spaces 21 between the spokes 17 provide a passage for air to pass through the seal member 9.
  • a multi-layer film 25 fits within the area of the seal member 9 bounded by the peripheral wall 19 and inner wall 13.
  • the multi-layer film is made of two layers of polytetrafluoroethylene 27 sandwiched between two layers of an organic polymeric material such as polypropylene 29.
  • the multi-layer film 25 is ultrasonically welded at peripheral area 31 and inner area 33 producing a sealed multi-layer assembly.
  • the top layer 29 could have spaced apart openings to permit the inner film 27 to expand with minimum resistance or restriction.
  • the multi-layer film 25 may be fastened to the bottom 11 and the spokes 17 by welding, if desired, and by use of a fatty acid polyamide adhesive, such as hereinabove described. Two beads of the adhesive may be used.
  • One bead is placed around the periphery of the bottom 11 where it joins the inside of peripheral wall 19 and the second bead may be placed on the bottom 11 where it joins the inner upstanding wall 13.
  • concentric raised ridges 35 may be formed on the bottom 11 of the seal 9.
  • the multi-layer film 25 will then be secured between ridges 35 on the bottom 11 and the neutral cover 37.
  • the vented neutral cover 37 is made of stainless steel and has a pair of spaced apertures 39 therein to allow the passage of air into the cell.
  • the vented neutral cover 37 will fit within the area of the seal member 9 bounded by the peripheral wall 19.
  • a conductive nail 7, preferably made of brass and having a thinned portion 41, may be inserted into and through sub-assembly 5 to keep the parts together.
  • the dimensions of the several components of the sub-assembly 5 and of the overall cell may be varied to meet any particular size requirements for the type of cell being assembled.
  • the sub-assembly 5 is inserted into the bottom of the inverted cell as shown in Fig. 3.
  • the peripheral wall 19 of the seal member 9 insulates the neutral cover 37 from electrical contact with the container 4.
  • a bottom cover 58 is placed into the steel container 4 and is also insulated from contact with the container 4 by the peripheral wall 19 of seal member 9.
  • the bottom cover 58 makes electrical contact with the nail 7, or other suitable electrically conductive means, enabling the bottom cover 58 to become the second external terminal for cell 3.
  • the edge of the steel container 4, and of the sub-assembly 5, are then rolled to hold the upturned portion 60 of the bottom cover 58 locked in position on the bottom of the cell 3.
  • a gap 62 surrounds the bottom cover 58, separating it from contact with the container 4.
  • the bottom cover 58 contains three small apertures 64, one of which is shown in Fig. 3, spaced approximately 120° apart, which provide a passage for air to enter into the bottom of the cell 3.
  • the air may pass through the sub-assembly 5 and contact the top portion of the cathode 6 through the air passage 21.
  • the top cover 66 may be fastened to the container by welds 68 after the cathode is rammed into place. It may be added before or after this step as it is merely attached to the container 4.
  • Example A D-size air-assisted alkaline cells
  • Example B Similar cell lots (Sample B) were produced except that the seals for the cells were made with two layers of polypropylene ultrasonically welded to the polypropylene seal.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Gas Exhaust Devices For Batteries (AREA)
  • Sealing Battery Cases Or Jackets (AREA)
  • Hybrid Cells (AREA)
EP92309902A 1991-10-29 1992-10-29 Von Luft gestützte alkalische Zellen und dazugehörige Dichtungsanordnung Expired - Lifetime EP0540324B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US784337 1991-10-29
US07/784,337 US5229223A (en) 1991-10-29 1991-10-29 Air-assisted alkaline cell having a multilayer film seal assembly

Publications (3)

Publication Number Publication Date
EP0540324A2 true EP0540324A2 (de) 1993-05-05
EP0540324A3 EP0540324A3 (en) 1993-07-28
EP0540324B1 EP0540324B1 (de) 1998-12-30

Family

ID=25132129

Family Applications (1)

Application Number Title Priority Date Filing Date
EP92309902A Expired - Lifetime EP0540324B1 (de) 1991-10-29 1992-10-29 Von Luft gestützte alkalische Zellen und dazugehörige Dichtungsanordnung

Country Status (8)

Country Link
US (1) US5229223A (de)
EP (1) EP0540324B1 (de)
JP (1) JPH05242875A (de)
KR (1) KR100269729B1 (de)
CA (1) CA2080793A1 (de)
HK (1) HK1007091A1 (de)
SG (1) SG44538A1 (de)
TW (1) TW273052B (de)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999045603A1 (en) * 1998-03-06 1999-09-10 Eveready Battery Company, Inc. Collector assembly for an electrochemical cell including an integral seal/inner cover
WO2001054210A2 (en) * 2000-01-19 2001-07-26 The Gillette Company Air recovery battery
WO2002073715A1 (en) * 2001-03-07 2002-09-19 Rayovac Corporation Independent seal and vent for an electrochemical cell
US7238448B1 (en) 2000-04-26 2007-07-03 The Gillette Company Cathode for air assisted battery

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4325464A1 (de) * 1993-07-29 1995-02-02 Emmerich Christoph Gmbh Co Kg Akkumulator mit Kunststoffgehäuse
GB2327141B (en) * 1997-07-10 2001-07-25 Ind Accumulatori Spa Soc A lead-acid accumulator, particularly for motor vehicles
US6383674B1 (en) 1999-03-11 2002-05-07 Eveready Battery Company, Inc. Air-assisted electrochemical cell construction
US6265104B1 (en) 1999-08-13 2001-07-24 The Gillette Company Hot-melt seal for metal-air battery
US6270921B1 (en) * 2000-01-19 2001-08-07 The Gillette Company Air recovery battery
US6399243B1 (en) * 2000-04-06 2002-06-04 The Gillette Company Air recovery battery
US6257402B1 (en) 2000-04-06 2001-07-10 Eveready Battery Company, Inc. Package having vapor pressure control for batteries
JP3540243B2 (ja) 2000-04-24 2004-07-07 Necエレクトロニクス株式会社 半導体記憶装置
US6558828B1 (en) 2000-05-26 2003-05-06 Eveready Battery Company, Inc. Zn/air cell performance in extreme humidity by controlling hydrophobic layer porosity
US6509588B1 (en) 2000-11-03 2003-01-21 Cardiac Pacemakers, Inc. Method for interconnecting anodes and cathodes in a flat capacitor
US7479349B2 (en) 2002-12-31 2009-01-20 Cardiac Pacemakers, Inc. Batteries including a flat plate design
US7718027B2 (en) * 2005-05-11 2010-05-18 Cardiac Pacemakers, Inc. Method and apparatus for concurrent welding and excise of battery separator
US7901808B2 (en) 2005-11-02 2011-03-08 Cardiac Pacemakers, Inc. System and method for sealing battery separator
EP2529435B1 (de) 2010-01-29 2013-10-30 Eveready Battery Company, Inc. Verfahren zur herstellung einer elektrochemischen zelle mit einer katalytischen elektrode mit mangandioxid
US10396343B2 (en) 2015-05-05 2019-08-27 Cps Technology Holdings Llc Sealing patch for electrolyte fill hole
CN114744361B (zh) * 2022-04-14 2024-04-19 北京科易动力科技有限公司 顶针式防爆阀及具有其的电池包
CN114678651B (zh) * 2022-04-14 2024-04-19 北京科易动力科技有限公司 防爆阀及具有其的电池包

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1064629A (fr) * 1951-02-27 1954-05-17 Tech Gautrat Bureau Perfectionnements apportés aux cellules électrolytiques notamment aux cellules d'accumulateur
US3741812A (en) * 1971-11-03 1973-06-26 Esb Inc Battery having gas pervious liquid impervious member sealed over holein top
US4066822A (en) * 1976-09-28 1978-01-03 P. R. Mallory & Co. Inc. Self sealing microporous membrane for electrochemical cells and method of forming same
EP0182596A2 (de) * 1984-11-14 1986-05-28 Eveready Battery Company, Inc. Galvanische Zelle
EP0441592A2 (de) * 1990-02-09 1991-08-14 Eveready Battery Company, Inc. Von Luft gestützte alkalische Zellen

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE549963A (de) * 1955-02-28
US3214300A (en) * 1962-10-04 1965-10-26 Gould National Batteries Inc Pressure relief device for sealed electric cells
US3920475A (en) * 1974-03-21 1975-11-18 Faat Khatovich Nabiullin Alkaline galvanic cell
US4678725A (en) * 1983-05-11 1987-07-07 Matsushita Electric Industrial Co., Inc. Hermetically sealed storage battery
US4636446A (en) * 1985-11-15 1987-01-13 Cheng Kwang Storage Battery Co., Ltd. Stopper structure for storage battery container
US4664287A (en) * 1986-03-10 1987-05-12 Saft America, Inc. Vent for an electrochemical cell
DE3704536A1 (de) * 1987-02-13 1988-08-25 Varta Batterie Dicht verschlossenes galvanisches element
US4999264A (en) * 1989-11-24 1991-03-12 Duracell Inc. Aqueous electrochemical cell
US5051323A (en) * 1990-04-13 1991-09-24 Eveready Battery Company, Inc. Rollback inner cover

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1064629A (fr) * 1951-02-27 1954-05-17 Tech Gautrat Bureau Perfectionnements apportés aux cellules électrolytiques notamment aux cellules d'accumulateur
US3741812A (en) * 1971-11-03 1973-06-26 Esb Inc Battery having gas pervious liquid impervious member sealed over holein top
US4066822A (en) * 1976-09-28 1978-01-03 P. R. Mallory & Co. Inc. Self sealing microporous membrane for electrochemical cells and method of forming same
EP0182596A2 (de) * 1984-11-14 1986-05-28 Eveready Battery Company, Inc. Galvanische Zelle
EP0441592A2 (de) * 1990-02-09 1991-08-14 Eveready Battery Company, Inc. Von Luft gestützte alkalische Zellen

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999045603A1 (en) * 1998-03-06 1999-09-10 Eveready Battery Company, Inc. Collector assembly for an electrochemical cell including an integral seal/inner cover
WO2001054210A2 (en) * 2000-01-19 2001-07-26 The Gillette Company Air recovery battery
WO2001054210A3 (en) * 2000-01-19 2002-01-24 Gillette Co Air recovery battery
US6372370B1 (en) 2000-01-19 2002-04-16 The Gillette Company Air recovery battery
US7238448B1 (en) 2000-04-26 2007-07-03 The Gillette Company Cathode for air assisted battery
US7615508B2 (en) 2000-04-26 2009-11-10 The Gillette Company Cathode for air assisted battery
WO2002073715A1 (en) * 2001-03-07 2002-09-19 Rayovac Corporation Independent seal and vent for an electrochemical cell

Also Published As

Publication number Publication date
US5229223A (en) 1993-07-20
CA2080793A1 (en) 1993-04-30
TW273052B (de) 1996-03-21
EP0540324A3 (en) 1993-07-28
JPH05242875A (ja) 1993-09-21
KR930009150A (ko) 1993-05-22
KR100269729B1 (ko) 2000-10-16
EP0540324B1 (de) 1998-12-30
SG44538A1 (en) 1997-12-19
HK1007091A1 (en) 1999-04-01

Similar Documents

Publication Publication Date Title
EP0540324B1 (de) Von Luft gestützte alkalische Zellen und dazugehörige Dichtungsanordnung
EP0441592B1 (de) Von Luft gestützte alkalische Zellen
KR101131258B1 (ko) 밀봉식 전기화학 전지용 하우징
US5639568A (en) Split anode for a dual air electrode cell
KR101762968B1 (ko) 전기화학 전지용 폐쇄조립체
US5569551A (en) Dual air elecrtrode cell
US5328778A (en) Metal-air cells comprising collapsible foam members and means for minimizing internal pressure buildup
US5318861A (en) Electrochemical metal-air cell and electrically and mechanically rechargeable anodes for use therein
US5248568A (en) Blowout multilayer film seal assembly for galvanic cells
US5270128A (en) Air assisted alkaline cell
JPH0430147B2 (de)
CN109690811A (zh) 二次电池
JPH0757729A (ja) 二極電極,二極バッテリー及び電極製造方法
JP5054866B2 (ja) 電気化学電池のための低プロファイル通気性シール
US3489616A (en) Galvanic atmospheric-oxygen cell
GB2138200A (en) Cylindrical battery
JPS59224049A (ja) 電気化学電池
JP2021068492A (ja) 非水電解質二次電池
WO2009014691A1 (en) Electrochemical cell having polymeric moisture barrier
JP2000090892A (ja) 大電流放電用二次電池
JPH03219552A (ja) リチウム電池
JPH09298067A (ja) ニッケル水素積層形組電池
JPS58209860A (ja) 電池
Schumm Jr et al. DESIGN OF THE HEAVY DUTY CARBON-ZINC CELL
JPS5999683A (ja) 筒形空気電池

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): BE FR GB

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

EL Fr: translation of claims filed
AK Designated contracting states

Kind code of ref document: A3

Designated state(s): BE FR GB

17P Request for examination filed

Effective date: 19940127

17Q First examination report despatched

Effective date: 19950221

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): BE FR GB

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20081018

Year of fee payment: 17

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20100630

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20091102

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20101025

Year of fee payment: 19

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 20111028

Year of fee payment: 20

BE20 Be: patent expired

Owner name: *EVEREADY BATTERY CY INC.

Effective date: 20121029

REG Reference to a national code

Ref country code: GB

Ref legal event code: PE20

Expiry date: 20121028

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20121028